Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put
OVERVIEW Experienced Statistical Programmer with expertise in supporting multiple clinical studies through the development, validation, and delivery of high-quality statistical programming outputs. Proficient in SAS (Base SAS, SAS/STAT, and Macro Language) and CDISC standards, including SDTM,
OVERVIEW Experienced Statistical Programmer with expertise in supporting multiple clinical studies through the development, validation, and delivery of high-quality statistical programming outputs. Proficient in SAS (Base SAS, SAS/STAT, and Macro Language) and CDISC standards, including SDTM,
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put
Company – Global Business Services, India Department – Clinical Data Science Location – Bangalore, India Drive life-changing innovation through data, where your programming expertise transforms clinical trials into breakthrough therapies for millions. Your new role As
Job Overview: Assist with the overall safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support function to the client project pgroups or as stand- alone
. Team: Global Patient Safety Location: Bangalore, Novo Nordisk Global Business Services (GBS), India Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the postmarketing period; and may manage a team. Summary of Responsibilities: Undertake primary medical review of cases, including
At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and
Dealing with lifecycle management of pharmaceutical product and medical devices in Asia Pacific Markets including administrative and CMC variations, Labelling, Safety updates, and Annual reports. Work with Country LRA, Cluster Hub, Global CDRA, labelling team for
Role Description – Associate Manager – Medical Affairs – COE, Mumbai About Shalina Healthcare: Shalina Healthcare is one of the largest pharmaceutical companies in sub-Saharan Africa. For the last 40 years we have made it our
THE POSITION: The Medical Review Lead (MRL) is responsible for supporting the timely and compliant execution of product surveillance activities for client projects. The role involves oversight and contribution to aggregate reports (PADERs, PBRERs), Risk Management
Job Title: Medical Reviewer – Signal Detection Summary We are seeking an experienced Medical Reviewer with expertise in Signal Detection to play a critical role in pharmacovigilance operations, ensuring the ongoing safety and regulatory compliance of
At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Labeling Manager to join our team. Management of pharmaceutical drug product labeling across global market
Company Description We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe,
THE POSITION: The position supports Pharmacovigilance department as a key member primarily contributing to leading a team that comprises of aggregate report scientists and physician(s) involved in aggregate report writing and signal detection. ESSENTIAL DUTIES AND
Job Title: Medical Reviewer – Signal Detection Summary We are seeking an experienced Medical Reviewer with expertise in Signal Detection to play a critical role in pharmacovigilance operations, ensuring the ongoing safety and regulatory compliance of
Location: Remote (India) Employment Type: Full-Time PharmXL International is a global pharmacovigilance and regulatory consulting organization delivering high-quality drug safety and compliance solutions to pharmaceutical, biotechnology, medical device, and healthcare companies worldwide. As part of our
THE POSITION: This position supports of the Pharmacovigilance (PV) Department as both a key team member and contributor in the scheduling and development of aggregate safety reports, generation of project and safety or signal report specific
THE POSITION: The most important aspect of this position is to perform medical review, evaluation, and analysis of Individual Case Safety Reports (ICSRs), assisting clients with the safety data, compliance with pharmacovigilance (PV) legislation and guidance,